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Details

Stereochemistry ACHIRAL
Molecular Formula C6H10
Molecular Weight 82.1436
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,5-HEXADIENE

SMILES

C=CCCC=C

InChI

InChIKey=PYGSKMBEVAICCR-UHFFFAOYSA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2

HIDE SMILES / InChI

Molecular Formula C6H10
Molecular Weight 82.1436
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Transition-metal-promoted reactions of boron hydrides. 17. Titanium-catalyzed decaborane-olefin hydroborations.
2001 Dec 12
The structure of ionized 1,5 hexadiene in the gas phase.
2001 Jul
The effect of rigidity, shape, unsaturation, and length on the anesthetic potency of hydrocarbons.
2001 Jun
Cyclocopolymerization: a mechanistic probe for dual-site alternating copolymerization of ethylene and alpha-olefins.
2002 Apr 24
Preparation and cell growth inhibitory activity of [PtR(2)L(2)] (R=polyfluorophenyl, L(2)=diene, cyclohexane-1,2-diamine (chxn) or cis-(dimethyl sulfoxide)(2)) and the X-ray crystal structure of [Pt(C(6)F(5))(2)(cis-chxn)].
2002 Apr 28
Conformation-dependent state selectivity in O-O cleavage of ONOONO: an "inorganic cope rearrangement" helps explain the observed negative activation energy in the oxidation of nitric oxide by dioxygen.
2002 Aug 14
Convergent approach to pumiliotoxin alkaloids. Asymmetric total synthesis of (+)-pumiliotoxins A, B, and 225F.
2002 Aug 9
Synthesis of [n]- and [n.n]cyclophanes by using Suzuki-Miyaura coupling.
2002 Jul 26
Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation.
2003 Apr 17
Dissociative and associative mechanisms of cope rearrangements of fluorinated 1,5-hexadienes and 2,2'-bis-methylenecyclopentanes.
2003 Jun 4
Hydrosilylation of dienes by yttrium hydrido complexes containing a linked amido-cyclopentadienyl ligand.
2004 Aug 7
Balancing dynamic and nondynamic correlation for diradical and aromatic transition states: a renormalized coupled-cluster study of the cope rearrangement of 1,5-hexadiene.
2005 Mar 2
A joint study based on the electron localization function and catastrophe theory of the chameleonic and centauric models for the Cope rearrangement of 1,5-hexadiene and its cyano derivatives.
2005 Nov 15
Diastereomerically-specific zirconium complexes of chiral salan ligands: isospecific polymerization of 1-hexene and 4-methyl-1-pentene and cyclopolymerization of 1,5-hexadiene.
2006 Oct 11
Studies of the electron-promoted cope cyclization of 2,5-phenyl-substituted 1,5-hexadiene radical anions.
2007 Jan 19
Calculational and experimental investigations of the pressure effects on radical-radical cross combination reactions: C2H5+C2H3.
2007 Jul 26
Structure-activity relationship (SAR) for the gas-phase ozonolysis of aliphatic alkenes and dialkenes.
2008 Apr 7
Cyclopolymerization of Nonconjugated Dienes with a Tridentate Phenoxyamine Hafnium Complex Supported by an sp(3) -C Donor: Isotactic Enchainment and Diastereoselective cis-Ring Closure.
2009 Nov 19
Asymmetric Rh-catalyzed intermolecular hydroacylation of 1,5-hexadiene with salicylaldehyde.
2009 Oct
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:52:19 GMT 2023
Edited
by admin
on Fri Dec 15 17:52:19 GMT 2023
Record UNII
4MTZ4764FI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,5-HEXADIENE
Systematic Name English
.ALPHA.,.OMEGA.-HEXADIENE
Common Name English
DIALLYL
Common Name English
NSC-60690
Code English
BIALLYL
Common Name English
Code System Code Type Description
PUBCHEM
11598
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
PRIMARY
CAS
592-42-7
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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NSC
60690
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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FDA UNII
4MTZ4764FI
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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MESH
C545783
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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ECHA (EC/EINECS)
209-754-7
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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WIKIPEDIA
1,5-Hexadiene
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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EPA CompTox
DTXSID4049323
Created by admin on Fri Dec 15 17:52:19 GMT 2023 , Edited by admin on Fri Dec 15 17:52:19 GMT 2023
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